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Kallmann syndrome associated with complex chromosome rearrangement

✍ Scribed by Casamassima, Anthony C. ;Wilmot, Patrick L. ;Vibert, Betsy K. ;Shapiro, Lawrence R.

Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
351 KB
Volume
45
Category
Article
ISSN
0148-7299

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A 17-year-old boy with Kallmann syndrome had complex congenital heart disease that included double-outlet right ventricle, d-malposition of the great arteries, right aortic arch, and hypoplastic main pulmonary artery. He had neurosensory hearing loss and mental retardation. The 7 previously reported